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CAS 396131-82-1

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(3-Cyanomethylphenyl)boronic acid

Description:
(3-Cyanomethylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has a cyanoalkyl substituent. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. Its cyano group contributes to the compound's electronic properties, potentially enhancing its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, the presence of the boron atom provides unique properties, such as the ability to act as a Lewis acid. Overall, (3-Cyanomethylphenyl)boronic acid is a versatile building block in the synthesis of complex organic molecules and has potential applications in drug development and materials science. Safety precautions should be observed when handling this compound, as with all boronic acids, due to potential toxicity and reactivity.
Formula:C14H18BNO2
InChI:InChI=1/C14H18BNO2/c1-13(2)14(3,4)18-15(17-13)12-7-5-6-11(10-12)8-9-16/h5-7,10H,8H2,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccc(CC#N)c2)O1
Synonyms:
  • [3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]Acetonitrile
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